SCHEMBL2357072

SCHEMBL2357072

NC(=O)c1cccc(C(=O)c2c[nH]c3ncc(Cl)cc23)c1F

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CYP2C9 P11712 5/20 0.49
▸ BRAF P15056 5/20 0.49
▸ PAK1 Q13153 3/20 0.49
▸ BMPR1B O00238 1/20 0.49
▸ PLK4 O00444 1/20 0.49
▸ PIR O00625 1/20 0.49
▸ AURKA O14965 1/20 0.49
▸ DCLK1 O15075 1/20 0.49
▸ EPHB6 O15197 1/20 0.49
▸ RIPK2 O43353 1/20 0.49
▸ STK16 O75716 1/20 0.49
▸ OXSR1 O95747 1/20 0.49
▸ MAP4K4 O95819 1/20 0.49
▸ ABL1 P00519 1/20 0.49
▸ RAF1 P04049 1/20 0.49
▸ LCK P06239 1/20 0.49
▸ FYN P06241 1/20 0.49
▸ FES P07332 1/20 0.49
▸ CSF1R P07333 1/20 0.49
▸ YES1 P07947 1/20 0.49

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL2357075 0.88 BRAF (0.49) CYP2C9BRAFPAK1BMPR1BPLK4
SCHEMBL2351339 0.88 CYP2C9 (0.48) CYP2C9BRAFPAK1PLK4AURKA
SCHEMBL2353295 0.88 BRAF (0.53) CYP2C9BRAFPAK1RIPK2RAF1
SCHEMBL3705466 0.86 CYP3A4 (0.52) CYP2C9BRAFPAK1BMPR1BPLK4
SCHEMBL2883743 0.86 CYP2C9 (0.46) CYP2C9BRAFPAK1PLK4AURKA
SCHEMBL3506159 0.86 BRAF (0.51) CYP2C9BRAFPAK1PLK4AURKA
SCHEMBL2352247 0.85 BRAF (0.63) CYP2C9BRAFPAK1BMPR1BPLK4
SCHEMBL3507259 0.84 BRAF (0.55) CYP2C9BRAFPAK1BMPR1BPLK4
SCHEMBL3506669 0.84 AXL (0.58) CYP2C9PAK1PLK4AURKAABL1
SCHEMBL3507600 0.83 AAK1 (0.46) CYP2C9PAK1CYP3A4

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 5 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8470818-B2 Compounds and methods for kinase modulation, and indications therefor PLEXXIKON INC. (US) 2013-06-25 — — US claimed
EP-1893612-B1 PYRROLO [2, 3-B]PYRIDINE DERIVATIVES AS PROTEIN KINASE INHIBITORS PLEXXIKON INC (US) 2011-08-03 — — EP claimed
US-20100249118-A1 protein kinase modulators such as Propane-1-sulfonic acid [2,4-difluoro-3-(5-ethoxy-1H-pyrrolo[1,3-b]pyridine-3-carbonyl)-phenyl]-amide, used to regulate signal transduction cascades, involved in the control of physiological functions including cellular growth and proliferation; anticarcinogenic agents PLEXXIKON INC. 2010-09-30 — — US claimed
US-20120122860-A1 SOLID FORMS OF SULFONAMIDES AND AMINO ACIDS PLEXXIKON, INC. 2012-05-17 — — US disclosed
WO-2010129570-A1 SOLID FORMS OF SULFONAMIDES AND AMINO ACIDS PLEXXIKON, INC. (US) 2010-11-11 — — WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20100249118-A1 protein kinase modulators such as Propane-1-sulfonic acid [2,4-difluoro-3-(5-ethoxy-1H-pyrrolo[1,3-b]pyridine-3-carbonyl)-phenyl]-amide, used to regulate signal transduction cascades, involved in the control of physiological functions including cellular growth and proliferation; anticarcinogenic agents MAP4K1, MAP4K2, MAP3K1 CYP2C9 4869/4885BRAF 95/4885PAK1 113/4885
US-20120122860-A1 SOLID FORMS OF SULFONAMIDES AND AMINO ACIDS BRAF, RAF1, ARAF CYP2C9 2176/4885BRAF 1/4885PAK1 290/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.

Send feedback